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Chemical Structure| 2101-87-3 Chemical Structure| 2101-87-3

Structure of 2101-87-3

Chemical Structure| 2101-87-3

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Product Details of [ 2101-87-3 ]

CAS No. :2101-87-3
Formula : C7H7N3O
M.W : 149.15
SMILES Code : COC1=CC=C(N=[N+]=[N-])C=C1
MDL No. :MFCD00869579

Safety of [ 2101-87-3 ]

Application In Synthesis of [ 2101-87-3 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 2101-87-3 ]

[ 2101-87-3 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 85-44-9 ]
  • [ 2101-87-3 ]
  • [ 2142-04-3 ]
  • 2
  • [ 656-35-9 ]
  • [ 2101-87-3 ]
  • [ 1115300-86-1 ]
YieldReaction ConditionsOperation in experiment
48% With sodium methylate; In ethanol; at 0℃; To a stirred and ice-cooled solution of 1 -azido-4-methoxy-benzene (1 .000 g, 6.7046 mmol) and 2,4-difluoro phenyl acetonitrile (1 .27 g, 8.0455 mmol) in absolute ethanol (20 ml), an ice-cooled solution of sodium methoxide (0.543 g, 10.0569 mmol) in absolute ethanol (10 ml) is added drop-wise. The resulting reaction mixture is evaporated and the residue is dissolved in methylene chloride and washed with water, brine, dried over MgSO4, filtered and evaporated to afford ~2 g of crude material as brownish solid. This material is purified by crystallization from methylene chloride and petroleum ether, to obtain the title compound as brown solid (1 .10 g, 48% yield). M. p. 152-156.5C. LC-ESI-HRMS of [M+H]+ shows 303.1046 Da. CaIc. 303.105742 Da, dev. -3.8 ppm.
  • 3
  • [ 34846-90-7 ]
  • [ 2101-87-3 ]
  • methyl 1-(4-methoxyphenyl)-(1H)-1,2,3-triazole-4-carboxylate [ No CAS ]
  • 4
  • [ 2101-87-3 ]
  • [ 37972-24-0 ]
  • C13H11N5O [ No CAS ]
  • 5
  • [ 136827-57-1 ]
  • [ 2101-87-3 ]
  • [ 114046-25-2 ]
  • [ 3230-50-0 ]
 

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